Malonamamidine hydrochloride is a useful biochemical for proteomics research. A useful biochemical for proteomics research.
| Pubchem Sid | 488194276 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488194276 |
| Sonrisas canónicas | C(C(=N)N)C(=O)N.Cl |
| IUPAC Name | 3-amino-3-iminopropanamide;hydrochloride |
| InChIKey | MPRLIYNSZYJODI-UHFFFAOYSA-N |
| INCHI | 1S/C3H7N3O.ClH/c4-2(5)1-3(6)7;/h1H2,(H3,4,5)(H2,6,7);1H |
| Isómeros SMILES | C(C(=N)N)C(=O)N.Cl |
| WGK Alemania | 3 |
| Peso molecular | 137.57 |
| Reaxy-Rn | 3911763 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3911763&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Clase | Carboxylic acids and derivatives |
| Subclass | Carboxylic acid derivatives |
| Intermediate Tree Nodes | Carboxylic acid amides |
| Direct Parent | Primary carboxylic acid amides |
| Alternative Parents | Carboximidamides Carboxamidines Organic oxides Hydrochlorides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Primary carboxylic acid amide - Carboximidamide - Carboxylic acid amidine - Amidine - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Hydrochloride - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as primary carboxylic acid amides. These are compounds comprising primary carboxylic acid amide functional group, with the general structure RC(=O)NH2. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 J2522052 | Certificate of Analysis | Mar 19, 2026 | A136566 |
| E2607025 | Certificate of Analysis | Dec 11, 2025 | A136566 |
| L2525225 | Certificate of Analysis | Dec 11, 2025 | A136566 |
| L2525226 | Certificate of Analysis | Dec 11, 2025 | A136566 |
| L2525227 | Certificate of Analysis | Dec 11, 2025 | A136566 |
| F2403364 | Certificate of Analysis | Jun 14, 2024 | A136566 |
| E2315388 | Certificate of Analysis | Apr 18, 2023 | A136566 |
| G2109130 | Certificate of Analysis | Apr 18, 2023 | A136566 |
| G2109131 | Certificate of Analysis | Apr 18, 2023 | A136566 |
| G2109132 | Certificate of Analysis | Apr 18, 2023 | A136566 |
| Punto de inflamación (°C) | 144.6 °C |
|---|---|
| Punto de ebullición (°C) | 315.4°C at 760 mmHg |
| Punto de fusión (°C) | 174-176 °C |
| Peso molecular | 137.570 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 137.036 Da |
| Monoisotopic Mass | 137.036 Da |
| Topological Polar Surface Area | 93.000 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 98.400 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 2 |
| 1. Mingjing Jin, Chenpeng Xi, You Chen, Wenbin Yuan, Miao Zeng, Zhongliang Yan, Xueying Yang, Chuanyao Luo, Zhaojin Wang, Arui Huang, Xiaowei Xu, Chang Yan, Aung Ko Ko Kyaw, Jinhui Tong, Shi Chen, Wen-Hua Zhang, Zhengguo Xiao, Guang Yang, Tom Wu, Yang Bai. (2025) Bidentate Anchoring Enables Concurrent Grain Orientation and Lattice Strain Mitigation in Wide-Bandgap Perovskites for High-Performance All-Perovskite Tandem Solar Cells. ADVANCED MATERIALS, [PMID:41085129] [10.1002/adma.202513281] |
